EUROLAB laboratory provides testing and compliance services within the scope of JIS T 3210 standard. It specifies requirements and test methods to validate the design of empty sterile disposable hypodermic syringes, with or without a needle, made of plastic or other materials and intended for the aspiration and injection of fluids after they have finally been filled.
This standard does not provide the requirements for the batch version. Syringes are primarily for human use. The sterile syringes specified in this standard are designed for use immediately after filling and are not intended to contain medication for extended periods of time.
Includes syringes for use with insulin, disposable syringes made of glass, syringes for use with power-driven syringe pumps, syringes prefilled by the manufacturer, and syringes intended for storage after filling.
EUROLAB assists manufacturers with JIS T 3210 test compliance. Our test experts, with their professional working mission and principles, provide you, our manufacturers and suppliers, the best service and controlled testing process in our laboratories. Thanks to these services, businesses receive more effective, high-performance and quality testing services and provide safe, fast and uninterrupted service to their customers.
To get an appointment, to get more detailed information or to request an evaluation, you can ask us to fill in our form and reach you.
EUROLABreporting and certification activities, United Accreditation Foundation (UAF), Turkish Accreditation Agency (TÜRKAK) ve Enterprise Accreditation Foundation (EAF) based on the accreditation provided by the accreditation body. The Enterprise Accreditation Foundation (EAF) accreditation body is also a signatory of the United Nations (UN GLOBAL COMPACT) organization.
